Hypogonadism classification: Difference between revisions
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{{Hypogonadism}} | {{Hypogonadism}} | ||
{{CMG}} | {{CMG}} {{AE}} {{AEL}} | ||
==Overview== | ==Overview== | ||
Hypogonadism may be classified according to the etiological site into three subtypes namely primary, secondary or combined. Hypogonadism can also be classified according to the age into two adult and child onset disease. Also, it could be classified based on the causes into [[acquired]] or [[congenital]].<ref name="pmid23258624">{{cite journal| author=Rey RA, Grinspon RP, Gottlieb S, Pasqualini T, Knoblovits P, Aszpis S et al.| title=Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach. | journal=Andrology | year= 2013 | volume= 1 | issue= 1 | pages= 3-16 | pmid=23258624 | doi=10.1111/j.2047-2927.2012.00008.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23258624 }} </ref> | |||
==Classification== | ==Classification== | ||
*Based on the location, hypogonadism can be classified into: | |||
**Primary: [[gonads]] (ovaries or testes) are the primary source of the pathology. | |||
**Secondary (central): If the cause of the disease is the [[hypothalamus]] or [[Pituitary gland|pituitary]]. | |||
* | **Combined | ||
* | |||
* | |||
* | *Based on the age, hypogonadism can be classified into: | ||
** | **[[Childhood]] onset hypogonadism | ||
** | **[[Adult]] onset hypogonadism | ||
* | *Based on the causes of the disease, hypogonadism can be classified into: | ||
**[[Acquired]] hypogonadism | |||
**[[Congenital]] hypogonadism | |||
==References== | ==References== | ||
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{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Latest revision as of 14:57, 3 October 2017
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Hypogonadism Microchapters |
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Hypogonadism classification On the Web |
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Risk calculators and risk factors for Hypogonadism classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]
Overview
Hypogonadism may be classified according to the etiological site into three subtypes namely primary, secondary or combined. Hypogonadism can also be classified according to the age into two adult and child onset disease. Also, it could be classified based on the causes into acquired or congenital.[1]
Classification
- Based on the location, hypogonadism can be classified into:
- Primary: gonads (ovaries or testes) are the primary source of the pathology.
- Secondary (central): If the cause of the disease is the hypothalamus or pituitary.
- Combined
- Based on the age, hypogonadism can be classified into:
- Based on the causes of the disease, hypogonadism can be classified into:
- Acquired hypogonadism
- Congenital hypogonadism
References
- ↑ Rey RA, Grinspon RP, Gottlieb S, Pasqualini T, Knoblovits P, Aszpis S; et al. (2013). "Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach". Andrology. 1 (1): 3–16. doi:10.1111/j.2047-2927.2012.00008.x. PMID 23258624.